HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 19020608, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19020606 | HCID 19020606 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19020608 | HCID 19020608 | — |
Reaction Steps
In a manner analogous to that described in Example 5, 1.6 g of 1-(4-acetylaminobenzoyl)-4-[2-(4-bromophenyl)ethyl]-piperazine, dissolved in 15 ml DMF, are treated first with 0.2 g NaH in 10 ml DMF and then with 0.6 g methyl iodide in 5 ml DMF. The crude product is crystallised from ether. Thus 1-[4-(N-acetyl-N-methylamino)benzoyl]-4-[2-(4-bromophenyl)ethyl]-piperazine is obtained, m.p. 161°-162°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05321027 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-587834af7da34ee185e7f8b2b966954a |
| Source note | uspto-grants-1994_06 |